Engineered fluorescent dye labeled nucleotide analogs for dna sequencing

ABSTRACT

Engineered nucleotide compositions, having polymerase interacting components that improve the interactivity of the polymerase and the nucleotide, particularly for nucleic acid sequencing applications. Compositions include the interactive polymerases along with the nucleotide analogs. Kits, methods and systems are provided for analysis of nucleoc acid synthesis reactions.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims benefit of Provisional U.S. Patent ApplicationNo. 61/070,823, filed Mar. 26, 2008, the full disclosure of which ishereby incorporated herein by reference in its entirety for allpurposes.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH

Not Applicable.

BACKGROUND OF THE INVENTION

Genetic analysis is a fundamental tool in life sciences research,including, for example, pharmaceutical development, medical diagnostics,agriculture, and academic research toward understanding the basicoperation of life. A large number of tools have been developed tofacilitate such genetic analysis and manipulation, including, forexample, nucleic acid amplification and monitoring techniques, nucleicacid sequencing techniques, and expression profiling techniques.

Despite major advances in each of these areas over the past severaldecades, there always remains room for improvement of even the state ofthe art techniques. By way of example, recent advances in nucleic acidsequencing employ optical confinement techniques to provide the abilityto eavesdrop on polymerase enzymes as they incorporate labelednucleotide analogs in a template mediated primer extension reaction,providing a real-time monitoring of nucleic acid synthesis that isexploited to identify the sequence of nucleotides in the templatenucleic acid. The technique is used for the full range of geneticanalysis, including site specific sequencing, genotype analysis,re-sequencing, and de novo sequencing applications.

The ability to observe the real time synthesis of nucleic acids and soderive their sequences pushes the horizons of genetic analysis furtherback to expose other potential opportunities for improvements to geneticanalysis technology. The present invention identifies some of theseopportunities and provides a number of solutions.

BRIEF SUMMARY OF THE INVENTION

The present invention is generally directed to nucleotide analogs, andpreferably labeled nucleotide analogs that serve as substrates fornucleic acid polymerase enzymes. The nucleotide analogs of the inventionare generally characterized by having a polymerase interacting componentengineered into their structure, which polymerase interacting componentenhances the interaction between the polymerase and the analog. Inparticularly preferred aspects, the polymerase interacting component ispositioned within a linking component that links the nucleotide portionof the analog with the labeling portion of the analog, and is situatedas to be in interactive proximity to one or more amino acid residues ofthe polymerase enzyme, e.g., one or more residues in or near thecatalytic center of the polymerase enzyme.

In a first aspect, the invention provides nucleotide compositions thatcomprise the structure:

N—Y—F

wherein N is a nucleoside polyphosphate or analog thereof, F is adetectable label moiety, and Y comprises a polymerase interactinglinkage complex. Optionally, the Y group comprises structures:

where L₁ is a first linker group, P or P′ are a polymerase interactinggroup, L₂ is a second linker group, and X is a linking group.

In certain aspects, the compositions comprise the structures:

where R₁ through R₁₁ are independently selected from H, O, OH,positively charge groups and negatively charged groups.

In a related aspect, A nucleotide composition, comprising the structure:

N—Y—F

where N is a nucleoside polyphosphate group or analog thereof coupledthrough a phosphate group other than an alpha phosphate group, L is adetectable labeling group, and Y comprises a polymerase interactinglinkage complex having a polymerase interacting component selected fromphenyl, biphenyl, triphenyl and a coumarin derivative.

In a further aspect, the invention provides nucleotide compositions,comprising the structure:

N-L₁-P-L₂-F

wherein N is a nucleoside polyphosphate or analog thereof, L₁ is a firstlinker group, P is a polymerase interacting group, L₂ is a second linkergroup, and F is a detectable label moiety.

In still other aspects, the invention provides methods of monitoringpolymerase mediated, template dependent primer extension. Such methodscomprise providing a polymerase template primer complex, contacting thecomplex with a nucleotide composition, comprising the structure:

N—Y—F

wherein N is a nucleoside polyphosphate or analog thereof, F is adetectable label moiety, and Y comprises a polymerase interactinglinkage complex, and monitoring reaction of the nucleotide compositionwith the complex in a primer extension reaction by detecting a signalfrom the detectable label.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 provides a schematic illustration of a nucleic acid sequencingprocess.

FIG. 2 provides a three dimensional model image of a nucleic acidpolymerase active derived from a Phi29 bacteriophage.

FIG. 3 provides a schematic illustration of an exemplary compound of theinvention and its expected interaction with certain polymerase residues.

FIG. 4 provides a sequence alignment of a number of bacteriophagepolymerases illustrating conserved structure within their active sites.

FIG. 5 provides a schematic illustration of a compound of the inventionhighlighting the structural components thereof.

FIG. 6 schematically illustrates three compounds of the inventionincorporating three different hydrophobic polymerase interactingcomponents.

FIG. 7 illustrates a synthetic scheme for a compound of the invention.

FIG. 8 provides an exemplary synthetic scheme for coupling fluorescentdye moieties to the compounds of the invention.

FIG. 9 illustrates an alternative synthetic scheme for synthesizingcompounds of the invention.

FIG. 10 illustrates a synthetic scheme for compounds of the invention.

FIG. 11 schematically illustrates an exemplary system used in observingsequencing reactions.

FIG. 12 shows a set of comparative plots of compounds of the inventiontested against different polymerase variants.

FIG. 13 schematically illustrates an alternative compound configurationin which a polymerase interacting component is engineered into thelabeling moiety.

DETAILED DESCRIPTION OF THE INVENTION I. General

The present invention is directed to novel compositions that are usefulin nucleic acid synthesis reactions, and particularly such synthesisreactions exploited for the identification of sequence elements formnucleic acids. The compositions of the invention generally include novelnucleotides or nucleotide analogs, as well as combinations of suchnucleotides or nucleotide analogs with nucleic acid polymerases thatinteract with and are capable of incorporating such nucleotides ornucleotide analogs in a template mediated primer extension reaction.

The nucleotide compositions of the invention are generally characterizedby improved interactivity with a nucleic acid polymerase. In particular,the nucleotide compositions of the invention are typically engineered toprovide one or more of improved reaction kinetics (e.g., Km, Kcat,substrate specificity, substrate and/or product dissociation rates,specific label insensitivity, i.e., creating analogs that havesubstantially the same kinetic characteristics, regardless of thelabeling group included, and the like), or altered reactioncharacteristics for a given application, improved polymerase protectivecharacteristics, and others.

The advantages of such compositions are readily demonstrated withreference to their use in preferred sequence by incorporation processes.Briefly, such processes utilize a nucleic acid polymerase complexed witha template sequence and complementary polymerization primer. The complexis interrogated with labeled nucleotide analogs that, when incorporated,provide a signal event that can be detected, and is thus indicative ofincorporation. Different types of nucleotides, i.e., bearing differentbases, e.g., A, T, G or C, bear differentially detectable labels, suchas spectrally distinguishable fluorescent dyes, permitting detection ofa signal indicative of both their identity and incorporation.

For example, certain preferred applications rely upon single molecule,real-time sequencing by incorporation methods. These methods typicallyemploy a nucleic acid synthesis complex that includes a polymeraseenzyme, e.g., a DNA polymerase, a template sequence, and a primersequence that is complementary to at least a portion of the templatesequence. In typical primer extension reactions, the polymerase extendsthe primer sequence by incorporating additional nucleotides that arecomplementary to the next nucleotide in the underlying templatesequence. In the real-time monitoring processes used with the invention,the reaction employs four distinctively labeled nucleotides, e.g., eachlabeled with a distinguishable fluorescent label. The complexes are thenconfigured such that upon incorporation of a given base, acharacteristic optical signal is produced, that both signals anincorporation event and allows identification of the type of baseincorporated.

In some cases, this configuration involves the immobilization of thecomplex upon a solid support, such as a planar surface, e.g., of a glassslide or other substrate, and in particularly preferred aspects, withinan optically confined region on a supporting substrate, such that anincorporating nucleotide is observable for a period of time that ischaracteristic of that incorporation. In particular, upon incorporation,a labeled nucleotide will be retained within or proximal to the activesite of the enzyme. Examples of such optically confined regions includeregions at or near a surface of a transparent substrate that isilluminated using total internal reflection (TIRF) spectroscopy toilluminate only species that are very close to the substrate surface. Insuch systems, nucleotides that are being incorporated into a compleximmobilized within the illumination region at or near the surface, willbe preferentially illuminated, and as a result, distinguishable overother, non-incorporated molecules. Typically, the complexes are providedin a configuration that provides for the optical resolution ofindividual molecular complexes, to permit single molecule (or singlecomplex) elucidation of nucleic acid synthesis. Such single moleculeconfiguration may include providing complexes diluted over a surfacesuch that sufficient space is provided between the individual complexesto provide for optical resolution. Alternatively or additionally, it maycomprise immobilization of individual complexes in different confinedspaces, including, for example, optically confined regions as discussedbelow.

In other methods, the complex may be provided immobilized within anoptically confined structure, such as a zero mode waveguide (ZMW). SuchZMWs provide for an illumination region that is confined in threedimensions, as opposed to only one. In particular, a nanoscale apertureis provided through a metal cladding layer that is disposed over atransparent substrate, to define the “core” of the ZMW. This nanoscalewell structurally confines the illumination to the dimensions of thecore. Further, where the cross sectional dimensions of the core are inthe nanoscale regime of, e.g., between about 20 and about 500 nm, itwill not permit passage of light of a frequency higher than a cutofffrequency from passing through the core. Instead, light illuminating oneend of the core will be subject to evanescent decay through the core,resulting in a shallow illuminated region within the core, thusconfining the illumination in the third dimension. By immobilizing acomplex upon the transparent “floor” of the ZMW, one can selectivelyilluminate and observe interactions that occur at or around the complexwithout excessive interference from other reagents in the overallreaction mixture. The complex is then exposed to fluorescently labelednucleotide analogs that are preferably labeled upon a phosphate groupthat is released upon incorporation. This process is schematicallyillustrated in FIG. 1.

As shown in FIG. 1, a DNA synthesis complex 102, that includes apolymerase enzyme, a template sequence and a primer sequence, isprovided immobilized on the surface of a transparent substrate 104 thatforms the base of the zero mode waveguide (ZMW) 106. Upon illuminationthrough the transparent substrate 104 with light of an appropriateexcitation wavelength, a small volume of the ZMW 106 is illuminated ator near the surface of the transparent substrate 104, as indicated bydashed line 108. As fluorescently labeled nucleotide analogs 110 diffusein and out of the illumination volume, their fluorophores will beexcited and emit fluorescence, but only for a very brief period, shownas a brief spike 120 in the exemplary signal plot provided below eachpanel. However, upon retention by the polymerase enzyme in complex 102for incorporation, the nucleotide analog will reside within theillumination volume for much longer, and as a result, be detectable,shown as a flash in the schematic of the complex and as a prolonged orbroader signal event 122 in the corresponding signal plot. Uponincorporation, the fluorescent label that is disposed upon one of theterminal phosphate groups, e.g., beta, gamma or more distal phosphate,will be cleaved from the nucleotide and will diffuse out of theillumination volume rapidly, and will no longer contribute to thedetected fluorescence. By providing each type of nucleotide with adifferent, distinguishable fluorescent label, one can not only identifythe occurrence of a detection event, but also identify the type of baseincorporated within a sequence context. See, e.g., U.S. Pat. Nos.6,056,661, 7,052,847, 7,033,764, 7,056,676, 6,917,726, 7,013,154,7,181,122, 7,292,742, the full disclosures of which are incorporatedherein by reference in their entirety for all purposes.

In still other processes, nucleotides are used that bear one or bothcomponents of an energy transferring fluorescent dye pair. For example,in some cases, the nucleotide carries a quencher fluorophore on oneportion of the nucleotide, e.g., the base, while carrying an donorfluorophore on a portion of the nucleotide that is released uponincorporation, e.g., coupled to the portion of the phosphate chain thatis released. Upon incorporation and cleavage of the phosphate groupsfrom the incorporated nucleotide, the fluorophore on the releasedphosphate is no longer sufficiently proximal to the quencher to remainquenched, and a fluorescent signal results (See, e.g., U.S. Pat. Nos.6,255,083, 6,762,048, 7,229,799, the full disclosures of which areincorporated herein by reference in their entirety for all purposes).

In an alternative configuration, a donor fluorophore is providedproximal to the active site of the polymerase enzyme, e.g., coupled tothe protein, while the nucleotide bears an acceptor fluorophore on aportion that is cleaved away upon incorporation, e.g., the phosphatechain. The reaction is then illuminated with light of the donor'sexcitation wavelength. Upon incorporation, the donor and acceptor are insufficient proximity to affect energy transfer from the donor to theacceptor, resulting in a fluorescent signal. Following incorporation,the acceptor is released from the complex and moves out of proximity tothe donor (See U.S. Pat. Nos. 6,056,661, 7,052,847, 7,033,764 and7,056,676).

One can identify the fluorescent nucleotides that are incorporated basedupon their characteristic signal profile. For example, as noted above,in the case of systems employing optical confinements like zero modewaveguides, this typically includes a longer retention time in theillumination volume as compared to non-incorporated molecules, and freephosphate-label groups. Further, based upon the spectral characteristicsof the fluorescent signal, one can then identify the type of baseassociated with such incorporation events.

Because the basis of these processes is the interaction between apolymerase and nucleotides or nucleotide analogs during primerextension, improvements in that interaction will tend to lead toimprovements to the overall processes. For example improvements ofreaction kinetics between labeled nucleotides and the polymerase enzymecan provide faster incorporation, and/or longer residence times, as wellas better fidelity of the enzyme toward a correctly incorporatednucleotide. That interaction may be improved from one or bothdirections. In particular, one may direct modifications to thepolymerase and/or to the nucleotide reagents to affect this improvement.

In addition to providing improved reaction characteristics, the modifiednucleotide analogs of the invention can also provide other benefits inthe desired applications. For example, in some cases, the presence ofexcited fluorophores within an active site of an enzyme such as apolymerase, potentially can lead to damaging effects believed to stemfrom generation of reactive oxygen species resulting from thefluorophore being excited to and relaxing from a triplet state (See,e.g., published U.S. Patent Application No. 2007/0128133, the fulldisclosure of which is incorporated herein by reference in its entiretyfor all purposes). In certain preferred aspects, the modified nucleotideanalogs of the invention are configured to maintain the fluorophoredistal to the active site through its interactions with other portionsof the enzyme. Nucleotide structures for accomplishing this aredescribed in greater detail below.

II. Compositions

A. Compounds

As noted above, the compositions of the invention typically includemodified nucleotide analogs that provide for an enhanced interactionbetween the nucleotide analog and the polymerase enzyme through apolymerase interacting component of the compound. The nucleotidecompositions of the invention are generally characterized by having thegeneral structure:

N-L₁-P-L₂-F

where N comprises a nucleoside polyphosphate or an analog thereof(referred to hereafter as the “nucleoside polyphosphate” portion orcomponent); L₁ is a first linking group coupled to the 5′ phosphategroup, or its equivalent, of the nucleoside polyphosphate component; Pis a polymerase interacting component; L₂ is a second linking grouplinking the polymerase interacting component to the F group, which is alabeling group.

As used herein, the nucleoside polyphosphate portion of the compositionincludes typical nucleoside polyphosphates and deoxynucleosidepolyphosphates, including those that include naturally occurringnucleobase components, such as adenine, guanine, uracil, thymine, andcytosine. This includes typical nucleoside triphosphates adenosine,uridine, guanosine, and cytidine, as well as deoxynucleosidetriphosphates, including deoxynucleoside triphosphates, which includedeoxyadenosine, deoxyguaniosine, deoxythymidine, deoxycytidine anduracil. Also included are such nucleotides that include longer 5′phosphate chains, such as tetraphosphate, pentaphosphate, hexaphosphate,heptaphosphate, and longer phosphate chain analogs. Also included withinthis portion of the compositions are other nucleotide analogs, such aspeptide nucleic acid monomers (PNAs), locked nucleic acid monomers(LNAs), and the like.

The first linking group L₁ is generally any linking group or groups thatcouple the 5′ portion of the nucleoside polyphosphate portion to thepolymerase interacting component “P”. Such linkages may includeindividual atoms such as O, N, S, or the like, or may even be a chemicalbond, e.g., a single, double or triple bond. Alternatively, andpreferably, longer linkages may be employed, such as alkyl, aminoalkyl,alkoxyl, aryl, polyaryl, or multimeric linker groups, such as nucleicacid linkers, peptidyl linkers, polyethylene glycol linkers, or otherappropriate linkages.

The polymerase interacting component of the compositions of theinvention includes molecular groups that interact with correspondingproximal groups on the polymerase enzyme during primer extension.Nucleic acid polymerases, as evidenced by their activity for commonsubstrates, nucleotides (including deoxy- and dideoxynucleotides), alsoshare a number of structural characteristics, particularly within oraround their active sites. For example, a number of polymerases derivedfrom bacteriophages share a number of conserved structural traits,particularly in residues that are proximal to the active site in thethree dimensional structure of the protein. By way of example, thecatalytic center of a DNA polymerase 200, shown as a three dimensionalmodel structure in FIG. 2, includes two hydrophobic residues at andaround the 375 and 512 positions, 202. Both of these regions fall withininteractive distance of a nucleotide analog 204 retained within theactive site pocket of the polymerase, and particularly a hydrophobiclabeling group on that analog. Typically, interactive distances, forpurposes of, e.g., Van der Waals interactions, will fall in the range offrom about 3 to about 5 angstroms between the polymerase interactingcomponent and those portions of the polymerase with which theinteracting component interacts. By configuring an analog with apolymerase interacting component that interacts with one or more of thespecific charge distribution or hydrophilic or hydrophobic nature ofthese regions, one would expect to enhance the interactivity between theanalogs and the polymerase.

In a particular exemplary system including certain modified orengineered polymerases, residues that correspond with the generalpositions described above, have been modified to include hydrophobictyrosine residues (See published U.S. Patent Application No.2007/0196846, incorporated herein by reference in its entirety for allpurposes). In this case, complementary or interacting hydrophobic groupsare employed in the nucleotide at the polymerase interacting component.

Based upon the foregoing, it will be appreciated that the polymeraseinteracting component (P or P′) may vary depending upon the threedimensional structure of the polymerase enzyme being employed. Ingeneral, however, such interacting components will comprise one or moreof positively charged groups, negatively charged groups, hydrophobicgroups, hydrophilic groups, and/or hydrogen bonding groups, dependingupon the specific structure of the polymerase being employed.

By way of example, where a polymerase includes positively charged groupsmost proximal to the polymerase interacting component when the analog iswithin the active site of the enzyme, the polymerase interactingcomponent may comprise a negatively charged group to provide an enhancedinteraction between the polymerase and the nucleotide analog. Someexemplary charged groups that could be incorporated into the nucleotidecompositions of the invention include, e.g., positively charged groupssuch as guanidinium, ammonium, iminium, oxonium or the like, and/ornegatively charged groups, such as carboxyl, phosphate, phosphonate,thio, sulfate, sulfonate, thioate, phosphothioate groups, and the like.

Likewise, where the polymerase includes hydrophobic moieties that aremost proximal to this portion of a nucleotide analog during binding,then the interactive group of the nucleotide analog will typicallyinclude hydrophobic groups to favorably interact with their counterpartson the polymerase. A variety of different hydrophobic groups can beincorporated into the general structure of the nucleotide analog shownabove, including, e.g., alkyl, aryl (including polyaryl groups),heteroaryl, cycloalkyl, bicycloalkyl, and other groups. Examples ofpreferred hydrophobic groups include phenyl groups, biphenyl groups ortriphenyl groups, heteroaryl groups and the like. A general structure ofa preferred biphenyl polymerase interacting component is illustrated bythe following structure:

where R₁ through R₆ are independently selected from H, O, OH, positivelycharge groups such as guanidinium, ammonium, iminium, oxonium or thelike, and/or negatively charged groups such as carboxyl, phosphate,phosphonate, thio, sulfate, sulfonate, thioate, phosphothioate groups,and the like. Similarly, a general structure of an exemplary heteroarylstructure includes a coumarin derivative polymerase interactingcomponent, such as a chromene, 2-chromanone, 2H-chromene, or2H-chromen-2-none. One exemplary polymerase interacting component hasthe general structure:

As with the biphenyl group illustrated previously, the side chainsubstituents of the polymerase interacting component shown above (i.e.,R₇ through R₁₁), are generally independently selected from the groupsset forth for groups R₁ through R₆, above. For certain polymeraseenzymes, e.g., those having two tyrosine residues proximal to the activesite (as set forth above), enhanced interactivity is produced byproviding a negatively charged group, such as SO₃, PO₃, OH, or the like,or a hydrogen bonding group, e.g., double bonded 0, at the R₁₁ positionto yield improved interactivity and thus improved reactioncharacteristics.

As above, where the polymerase molecule possesses hydrophilic moietiesat these points, then similarly hydrophilic groups may be employed inthe polymerase interacting component on the nucleotide analog, e.g.,amine, carboxyl, guanidinium, thioates, etc.

While generally described as being either hydrophobic, charged, or thelike, it will be appreciated that the polymerase interacting componentmay comprise more than one basis of interactivity with the polymerase,including, for example, charged hydrophobic groups, groups with variablelocal charge distributions, e.g., both positive and negative, and thelike.

In the structures illustrated above, the polymerase interactingcomponent is linked to the labeling group F through linking group L₂.Again, linking group L₂ may be selected from any of a variety ofdifferent types of linking groups, as with L₁, above. In preferredaspects, adjustable length linking groups are used to provide linkage ofthe labeling group to the rest of the compound, such as alkyl, aryl,peptidyl, or oligonucleotide based linkages. For example, in certainpreferred aspects, methyl, ethyl, butyl, propyl, pentyl, hexyl, orlonger chain alkyl groups are employed as the second linking group, thusallowing facile modification of the distance of the labeling group fromthe polymerase interacting component. The linker groups may be coupledthrough any conventional linkage technique, including, for example, anamide linkage generated through standard NHS chemistry (see below).

Although generally illustrated in a serial linkage, e.g., -L₁-P-L₂-F, itwill be appreciated that the polymerase interacting component mayinclude a linkage component between L₁ and L₂ that does not, itselfprovide for interaction with the polymerase. As such, the foregoingstructure encompasses the structure where the interacting portion of thepolymerase interaction component may be provided as a side chaincomponent, such as in the partial structure illustrated below:

where X is a linkage component of the polymerase interacting componentand P′ is the portion of the polymerase interacting component thatfunctionally interacts with the polymerase enzyme, e.g., X and P′together make up the “P” group from the linear structure set forthabove.

Based upon the foregoing, therefore, one may schematically illustratethe structure of certain compounds of the invention as:

N—Y—F

where Y comprises a polymerase interacting linkage complex that joinsthe nucleotide component to the labeling component, and may be forexample, the L₁-P-L₂ or L₁-X(P′)-L₂ structure illustrated above.

FIG. 3 provides a schematic illustration of a compound of the inventionthat includes a triphenyl group within the polymerase interactingcomponent in conjunction with the predicted location of the two tyrosineresidues of the modified polymerase enzyme.

As will be appreciated from the present disclosure, polymeraseinteracting components will typically be positioned to be appropriatelyproximal to the portions of the polymerase with which interaction issought, e.g., charged or hydrophobic residues around he active site ofthe polymerase. Restated, the linkage between the nucleosidepolyphosphate component of the compound and the polymerase interactingcomponent will typically be selected to appropriately position theinteracting component sufficiently proximal to the particular residuesin the polymerase to provide functional interaction, e.g., higheraffinity, leading to better reaction kinetics. For example, in the caseof the polymerase structure illustrated in FIG. 2, it is expected thatthe requisite distance from the nucleoside component to the polymeraseinteracting component will typically be from about 20 to about 40angstroms. Factoring in the length of each phosphate group(approximately 2.72 angstroms), the polyphosphate chain may account forfrom about 8.16 angstroms to about 19.04 angstroms of this distance,depending upon whether a nucleoside tri-, tetra-, penta-, hexa- or evenheptaphosphate is used as the nucleoside polyphosphate component. Inpreferred aspects, a tri, tetra, penta or hexaphosphate is used, so thatthe phosphate distance is approximately 8.16, 10.88, 13.60 or 16.32angstroms, respectively. Accordingly, linking group L₁ will typically beselected to make up for the remaining desired distance, e.g., from about4 to about 32 angstroms.

For many polymerase enzymes for which the three dimensional structurehas been elucidated, the distance between the active site andpotentially interacting residues is expected to be approximatelyequivalent to the modeled structure shown in FIG. 2, such that adistance between a nucleoside component and a polymerase interactingcomponent of between about 20 angstroms and about 40 angstroms, andpreferably, 20 to 30 angstroms, will be applicable. For example, forcertain polymerases described elsewhere herein, e.g., phi29 or otherpolymerases, the distance between the nitrogen of a nucleobase in aretained nucleotide and the residues identified elsewhere herein isapproximately 27 angstroms, based upon three dimensional models of theenzyme.

As noted above, the present invention provides compositions that includenucleotide analogs that desirably interact with the polymerase enzymeswith which they are reacting through the inclusion of a polymeraseinteracting component in the nucleotide analog compound. As noted above,the nature of the interacting component will depend upon the portions ofthe polymerase enzyme with which it interacts. For example, the activesites of polymerase enzymes will often include a number of conservedfeatures, such as a binding groove, trough or funnel in which sits thetemplate primer complex during synthesis. In a specific example, anumber of bacteriophage derived polymerases share some common structuralcharacteristics at positions proximal to the active site. For example,FIG. 4 shows a sequence alignment among five different bacteriophagepolymerases (B103, M2, GA1, Phi29, and B. subtilis phage PZA. See Meijeret al., Microbiol Mol Biol Rev. 2001 June; 65(2): 261-287). Just lookingat those residues that correspond in position to those noted above (375and 512), one can readily observe common charge characteristics amongthe various polymerases. In particular, these residues are charged andhydrophilic, and are predominantly negatively charged at the 375 residueand positively charged at the 512 residue. Accordingly, it would beexpected that common polymerase interacting components may be readilyemployed for each of these types of polymerases. In particular, one mayprovide a bifunctional interacting component, e.g., being partiallycharged at one end and oppositely charged at the other end, oralternatively, bearing hydrophobic moieties at one end while providinghydrophilic moieties or charge moieties at the other end. Further,identification off other common interacting features around the activesite can provide additional avenues for interactivity.

While the general structure of the compounds of the invention isdescribed above, specific exemplary structures are provided below. Inparticular, the structures of the nucleoside polyphosphate portion ofthe compound will typically comprise a nucleobase portion coupled to asugar moiety, such as a ribosyl group at the 1′ position, and a 5′phosphate chain that may include 3, 4, 5, or more phosphate groups. Anexemplary nucleoside polyphosphate structure includes:

where R₁ and R₂ are independently selected from H and OH, and R₁ ispreferably OH; Base is a nucleobase selected from adenine, guanine,thymine, cytosine, uracil, inosine and the like; n is 2 or greater, andpreferably is selected from 2, 3, 4, 5 or 6. Although illustrated as O⁻,the substituents on each of the phosphate groups present are alsooptionally independently selected from other groups such as BH₃ and S.

The linking groups L₁ and L₂, that link the nucleoside polyphosphateportion of the molecule to the polymerase interacting component, or thepolymerase interacting component to the labeling group may independentlycomprise single bonds, single atoms or larger molecules. For example L₁and L₂ may be independently selected from O, N, S, or the like, or theymay include larger structures, such as alkyl, aminoalkyl, alkoxyl, aryl,polyaryl, or multimeric linker groups, such as or other larger linkages.Multimeric linkages are also envisioned as linking groups for one orboth of L₁ and L₂, including, e.g., vinyl groups, nucleic acid linkers,peptidyl linkers, polyethylene glycol linkers, polybenzyl or otherpolyaryl groups, or other appropriate linkages. In preferred aspects,the linking groups L₁ and L₂ will be independently selected fromindividual atoms, such as O, N or S, alkyl groups of from 1 to 18carbons in length, including substituted alkyl groups, such asaminoalkyl linkers. Optionally, alkoxy groups of from 1 10 18 carbonsare employed as linkers. In certain exemplary embodiments, aminohexylgroups are employed as linkers alone or in conjunction with longeralkoxy groups, such as aminohexyl-aminoheptanoic acid linkers or thelike. As will be apparent from the instant disclosure, one can employ avariety of linker chemistries in coupling the various groups of thecompound of the invention together.

The labeling group F is typically a readily detectable labeling group,such as a luminescent, fluorescent, fluorogenic, chromogenic, magnetic,radioactive or other type of detectable label. In preferred aspects, thelabeling group F is selected from fluorescent labeling groups includingindividual fluorophores and cooperative fluorophores, e.g., one or bothmembers of a donor-quencher or FRET pair. In the case where F is atleast one member of a cooperative fluorophore pair, the second member ofthe pair may also be included within the F group, e.g., as a unifiedFRET dye structure (See, e.g., U.S. Pat. No. 5,688,648 for a discussionof FRET dyes), or it may be provided elsewhere on the analog or theoverall system. For example, in some cases, the other member of the pairmay be coupled to and as a portion of the Base moiety attached to thesugar group (See, e.g., U.S. Pat. No. 6,232,075 previously incorporatedherein by reference). Alternatively, the other member of the pair may becoupled to another reaction component, e.g., a polymerase enzyme (See,e.g., U.S. Pat. No. 7,056,676, previously incorporated herein byreference).

A wide variety of different types of fluorophores are readily availableand applicable to the compounds of the invention and includefluorescein, or rhodamine based dyes, cyanine dyes and the like. Avariety of such dyes are commercially available and include the Cy dyesavailable from GE Healthcare (Piscataway, N.J.), such as Cy3, Cy5, andthe like, or the Alexa® family of dyes available fromInvitrogen/Molecular Probes (Carlsbad, Calif.), such as Alexa 488, 500,514, 532, 546, 555, 568, 594, 610, 633, 647, 660, 680, 700, and 750.These fluorophores may be present as individual fluorophores or they maybe present in interactive pairs or groups, e.g., as fluorescent resonantenergy transfer (FRET) pairs.

Alternative labeling strategies may employ inorganic materials aslabeling moieties, such as fluorescent or luminescent nanoparticles,e.g. nanocrystals, i.e. Quantum Dots, that possess inherent fluorescentcapabilities due to their semiconductor make up and size in thenanoscale regime (See, e.g., U.S. Pat. Nos. 6,861,155, 6,699,723,7,235,361). Such nanocrystal materials are generally commerciallyavailable from, e.g., Invitrogen, Inc., (Carlsbad Calif.). Again, suchcompounds may be present as individual labeling groups or as interactivegroups or pairs, e.g., with other inorganic nanocrystals or organicfluorophores.

Again, the labeling group may be directly coupled to the polymeraseinteracting component, e.g., the hydrophobic group, or it may be coupledthrough a longer linking group. Such linking groups include thosedescribed above, such as alkyl, aryl, peptidyl, and the like, as well asthe aforementioned multimeric linking groups.

FIG. 5 schematically illustrates one exemplary compound of the inventionalong with a legend indicating the different constituent components. Inparticular, the compound shown provides a nucleoside polyphosphatecomponent 502 that is comprised of a deoxythymidine pentaphosphate. Thenucleoside polyphosphate component 502 is linked, via an aminohexyllinking group 504 to the polymerase interacting component 506, shown asa triphenyl group. This triphenyl group is, in turn, coupled to afluorophore 510 via another alkyl linker group 508.

FIG. 6 illustrates a side by side comparison of nucleosidehexaphosphates having aminohexyl aminoheptanoic acid linkers couplingthe nucleoside to different hydrophobic polymerase interactingcomponents. In particular shown are compounds that includes a benzylgroup (compound 602), a naphthyl group (compound 604), and an anthracylgroup (compound 606).

FIG. 7 schematically illustrates the synthesis scheme for the compoundillustrated as compound 602 in FIG. 6. In particular, as shown, areaction of benzoic acid (1) with 1,1′-carbonyldiimidazole (CDI) andN-hydroxysuccinimide (NHS) in DMF gave the activated benzoyl NHS ester(2) which is then reacted with aminocaproic acid to give the couplingproduct (3). Again, activation using the CDI/NHS chemistry gave theactivated NHS ester (4) which is then reacted with aminohexyldeoxynadenosine hexaphosphate to give the target product,benzene-XX-dA6P (5).

FIG. 8 provides an exemplary synthetic scheme for coupling fluorescentdyes to an exemplary compound (compound 602). Again, as shown, areaction of aminomethylbenzoic acid (1) with TFA-NHS provides the TFAprotected NHS activated ester (2) which is then reacted with aminohexyldeoxynadenosine hexaphosphate to give the adduct (3). Deprotection ofthe adduct (3) with ammonium hydroxide gives the amino nucleotide (4).Reaction of (4) with Alexa488-TFP in 0.1 M NaHCO₃ buffer solution givesthe dye labeled nucleotide (5) after HPLC purification.

An alternative synthetic scheme is illustrated in FIG. 9 for generationof a dye labeled nucleotide analog having a biphenyl or napthylpolymerase interacting component. As shown, activation ofnaphthalene-1,4-dicarboxylic acid (1) with CDI/NHS gives the bis-NHSester (2), which is then reacted with one equivalent of mono Bocprotected 1,6-hexanediamine to give the mono adduct (3). Deprotection ofBoc group with 3M HCl in a 1:1 water:MeOH solution gives the aminoacid(4). Protection of the amino group and activation of the carboxylic acidgroup can be done with the TFA-NHS reagent to give the activated ester(5), which is then reacted with aminohexyl deoxyadenosine hexaphosphatefollowing by the ammonium hydroxide deprotection to give the adduct (7).Reaction of the amino compound (7) with Alexa488-TFP in 0.1 M NaHCO₃buffer solution gives the dye labeled nucleotide, compound (8), afterHPLC purification.

An exemplary compound of the invention is provided by the structure:

where R₁ through R₆ are as described above. As will be appreciated,these groups may generally be modified to adjust the electrostaticinteraction by substituting one or more of these groups with electronrich or poor groups to interact with specific residues for thepolymerase enzyme being used. L₁ may comprise a direct bond between theterminal oxygen and the aromatic interacting component, or it maycomprise multiple atoms, such as in a simple alkyl linkage of variablelength, PEO linkers, PEG linkers or any of a variety of other linkergroups. Likewise the linker between the labeling component F and thearomatic interacting component may be comprised of any of a variety ofdifferent linker types. As above, the label group (F) comprises adetectable labeling group, such as a fluorescent or luminescent labelinggroup, or alternatively, an electrochemically detectable group, such asa charged or magnetic moiety, particle or the like. Fluorescent labelinggroups are generally preferred for the ease of detection, high quantumyield, and ease of linking with nucleotide compounds. Such fluorescentcompounds include small molecule fluorophores, as well as particle basedfluorescent groups, such as semiconductor nanocrystals, or otherfluorescent or fluorogenic particles. As will be appreciated, the basewill typically comprise any nucleobase, and prefereably nucleobasesassociated with ribonucleotides and deoxyribonucleotides. Also, whileillustrated as a triphosphate compound, it will be appreciated thatpolyphosphates with more than three phosphate groups are also envisionedin the context of the invention, e.g., where n is 1 or greater, e.g., 1,2, 3, 4, 5 or greater. Likewise, although illustrated as PO₃ groupswithin the polyphosphate chain, it will be appreciated that the oxygenside chains may be substituted with any of a number of other groups, andstill fall within the scope of the invention. For example, oxygen sidegroups may generally be substituted with a variety of other groups, suchas sulfur, boron, or others, while still allowing their use assubstrates for polymerase enzymes.

In alternate cases, one may substitute the biphenyl polymeraseinteracting component with a coumarin group to yield, e.g., thecompound:

FIG. 10 provides an exemplary synthetic scheme for the compoundillustrated above. Activation of 7-hydroxycoumarin-4-acetic acid (9)with CDI/NHS followed by reaction with ethylenediamine and subsequentprotection of the amino group gives the hydroxycoumarin (10). Reactionof (10) with POCl₃ and then pyrophosphate gives the correspondingtriphosphate (11). Again, activation of (11) with CDI and reaction withdATP followed by ammonium hydroxide deprotection gives theamino-cumarin-dA6P (12). Reaction of amino-cumarin-dA6P (12) withfluorescent dye A488-TFP gives the dye labeled nucleotide, compound(13), after HPLC purification.

While described in terms of the label component and the polymeraseinteracting component as being separate and discrete groups within theoverall structure of the compounds of the invention, it will beappreciated that certain aspects of the invention may include polymeraseinteracting components in the label portion itself. In particular, asmany fluorescent compounds are larger molecules, they providesignificant opportunity to adjust local properties of the overallcompound. By way of example, a labeled compound may be provided thatincludes polymerase interacting functionality integrated into the dye orlabel molecule. Such interacting capability includes those describedabove, e.g., hydrophobicity, charge (positive and/or negative), andbifunctional characteristics. Examples of bifunctional characteristicsintegrated into a labeling component are shown in, e.g., FIG. 13. Inparticular, shown are two fluorescently labeled nucleotide analogs, inwhich charged moieties (sulfonate groups) are coupled to portions of thelabel that would be expected to interact with oppositely chargedpolymerase components. As shown, the top compound (Panel I) includes adoubly charged labeling compound, while the second compound (panel II)includes 3 charged groups.

B. Compound/Polymerases

The compounds of the invention are typically applied in conjunction withother reaction components, but particularly with their complementarypolymerase enzymes. As used herein, a complementary polymerase enzymefor a given embodiment of the compounds of the invention is a polymerasethat includes a portion that interacts with the polymerase interactingcomponent of the compound, when that compound is retained within theactive site of that polymerase.

By way of example, for the compound illustrated in FIG. 3, onecomplementary polymerase enzyme would be that shown in FIG. 2, havingtwo tyrosine moieties disposed at the 375 and 512 positions, andproximal to the triphenyl group of that nucleotide analog when it isretained within the active site (as shown in FIG. 3), giving rise to adesirable hydrophobic interaction between the analog and the polymerase.Moreover, other complementary polymerases for the nucleotide analogshown in FIG. 3, or those nucleotide analogs having other hydrophobicpolymerase interacting groups, will also typically possess hydrophobicresidues at similar locations in the three dimensional structure of thepolymerases' active site.

In contrast, complementary polymerases to nucleotide analogs that havepositively or negatively charged groups in the position of thepolymerase interacting component may generally have oppositely chargedgroups proximal to such position on the nucleotide analog, when thatanalog is retained within the active site of the polymerase.

As will be appreciated, the compositions of the invention may generallybe broadly useful in a range of different polymerase systems. Forexample, as noted above, reactions employing phage derived polymerases,such as Φ29 DNA polymerase or mutant thereof, may be benefited from theuse of the compositions described herein. Other polymerases include, forexample, Taq polymerases or derivatives thereof, DNA Pol I polymerasesand its derivatives, T7 polymerases, an RB69 polymerase, T5 polymerases,or a polymerase corresponding to a Klenow fragment of a DNA Pol Ipolymerase, as well as other polymerases that share homologous sequencesand/or active site structures. For example, the recombinant DNApolymerase can be homologous to a wild-type or exonuclease deficient Φ29DNA polymerase, e.g., as described in U.S. Pat. No. 5,001,050,5,198,543, or 5,576,204. Similarly, DNA polymerases can be homologous toΦ29, B103, GA-1, PZA, Φ15, BS32, M2Y, Nf, G1, Cp-1, PRD1, PZE, SFS,Cp-5, Cp-7, PR4, PR5, PR722, or L17, or the like.

As noted above, the reaction compositions of the invention will alsotypically include additional components for optimizing reactionconditions, including, e.g., buffers, salts, divalent metal ions, e.g.,Mg++ and/or Mn++.

III. Methods

The compositions of the invention are particularly suited to analyticalapplications employing polymerase mediated nucleic acid synthesis,including, for example, real time nucleic acid amplification processesand nucleic acid sequencing by incorporation processes. Examples ofnucleic acid sequence by incorporation processes are described, forexample in U.S. Pat. No. 6,210,891, which describes a sequencing processin which incorporation is detected through the enzymatic identificationof pyrophosphate released from an incorporated nucleotide. As will beappreciated, the compounds of the invention would provide a facilemechanism for the fluorescent detection of released pyrophosphate, basedupon the labeling moieties used for the nucleotide analogs. Morepreferred methods employ the real time identification of incorporationevents, including identification of the type of nucleotide analogincorporated (i.e., A, C, G, or T), as described above.

In the context of the invention, the compounds of the invention areprovided to the complex that comprises a complementary polymerase enzyme(as described above) for the given analog structures. Uponincorporation, the polymerase retains the nucleotide analog in itsactive site, giving rise to a fluorescent signal associated withincorporation, e.g., based upon enhanced retention time within anillumination volume, generation of an unquenched fluorescent group,bringing a complementary FRET pair into sufficient proximity, or thelike. The nature of the fluorescent signal is indicative of bothincorporation, and the type of nucleotide incorporated. The fluorescentsignals are detected and evaluated in order to give rise to a calledbase in the overall sequence of the template (See, e.g., U.S. PatentApplication No. 60/933,399, the full disclosure of which is incorporatedherein by reference in its entirety for all purposes).

IV. Systems

The systems of the invention typically employ those types of fluorescentdetection schemes described in, e.g., Published U.S. Patent ApplicationNo. 2007/0188750, and copending. U.S. patent application Ser. No.11/901,273, filed Sep. 14, 2007, the full disclosures of which areincorporated herein by reference, in conjunction with the compositionsdescribed herein.

One exemplary system is shown in FIG. 11. As shown, the system 1000includes a substrate 1002 that includes a plurality of discrete reactionregions, e.g., reaction wells or optical confinements 1004 containingimmobilized polymerase/template/primer complexes. An excitation lightsource, e.g., laser 1006, is optionally provided in the system and ispositioned to direct excitation radiation at the various reactionregions 1004. This is typically done by directing excitation radiationat or through appropriate optical components, e.g., dichroic 1008 andobjective lens 1010, that direct the excitation radiation at thesubstrate 1002, and particularly the reaction regions 1004. Emittedfluorescence from the reactions, e.g., from incorporating nucleotides,in reaction regions 1004 are then collected by the optical components,e.g., objective 1010, and passed through additional optical elements,e.g., dichroic 1008, prism 1012 and lens 1014, until they are directedto and impinge upon an optical detection system, e.g., detector array1016. The signals are then detected by detector array 1016, and the datafrom that detection is transmitted to an appropriate data processingunit, e.g., computer 1018, where the data is subjected tointerpretation, analysis, and ultimately presented in a user readyformat, e.g., on display 1020, or printout 1022, from printer 1024.

V. Kits

The compositions of the invention are also typically provided in kitformat along with other useful components. For example, such other kitcomponents will typically include, in addition to the nucleotidecompositions described herein, appropriate buffers, salts and the like,as described above, as well as complementary polymerase enzymes, andoptionally primer sequences for the desired application. Such primersmay be specific to the identification of a known genetic sequence, e.g.,identifying specific genetic sequences, such as those associated withcertain pathologies, e.g., viral infections, bacterial infections,cancer cell types, and the like. Alternatively, for non-targetedsequencing applications, universal primer sequences may be included.

In the case of applications that employ specific detection strategies,e.g., TIRF based detection or ZMW based detection, the kits may alsoinclude appropriate substrates for carrying out the analysis. Forexample, the kits may employ a zero mode waveguide array within the kitthat may be pretreated to already include or be ready for immobilization

VI. Examples

Analogs that included hydrophobic polymerase interacting components weretested as substrates for four polymerase variants, each having atyrosine residues at the 375 and 512 positions, and compared againstother analogs that did not include hydrophobic polymerase interactingcomponents. The analogs tested were Alexa 680-Hex-O-dA6P, Alexa660-Hex-O-dA6P, Alexa 568-Hex-O-dT6P, Alexa 568-Hept-Hex-O-dT6P, Alexa680-Hex-O-dG6P, Alexa 647-Hex-O-dG6P, Alexa 555-Hept-Hex-dC6P, Alexa488-Hept-Hex-O-dC6P, Cy3B-Hept-Hex-O-dC6P, Anthr-Hex-Hex-O-dA6P, Alexa555-Hex-O-dG6P, Naph-Hex-Hex-O-dA6P, Alexa 647-Hex-O-dA6P, Alexa488-Hept-Hex-O-dA6P, Alexa 488-Hex-O-dC6P, where “Hex” denotes aaminohexyl linker and “Hept-Hex” denotes a aminohexyl heptanoic acidlinker.

The Km was determined for each enzyme analog combination and the resultswere plotted as the bar graphs shown in FIG. 12. The Hept-Hex linkersare denoted by the “15X” notation in the figure, while the othercompounds included an amino hexyl linker. As can be seen, both thecompound that included the Napthyl and anthracyl polymerase interactingcomponents showed improved kinetics in the form of lower Km valuesagainst each of the four enzyme variants.

Although described in some detail for purposes of illustration, it willbe readily appreciated that a number of variations known or appreciatedby those of skill in the art may be practiced within the scope ofpresent invention. All terms used herein are intended to have theirordinary meaning unless an alternative definition is expressly providedor is clear from the context used therein. For methods recited herein,to the extent that a composition of the invention is disclosed as beingprovided in a method step, it will be appreciated that disclosure ofsuch provision implicitly discloses the preparation of such compositionin a transformative fashion. To the extent any definition is expresslystated in a patent or publication that is incorporated herein byreference, such definition is expressly disclaimed to the extent that itis in conflict with the ordinary meaning of such terms, unless suchdefinition is specifically and expressly incorporated herein, or it isclear from the context that such definition was intended herein. Unlessotherwise clear from the context or expressly stated, any concentrationvalues provided herein are generally given in terms of admixture valuesor percentages without regard to any conversion that occurs upon orfollowing addition of the particular component of the mixture. To theextent not already expressly incorporated herein, all publishedreferences and patent documents referred to in this disclosure areincorporated herein by reference in their entirety for all purposes.

1-11. (canceled)
 12. A method of monitoring polymerase mediated,template dependent primer extension, comprising: providing a polymerasetemplate primer complex; contacting the complex with a nucleotidecomposition, comprising the structure:N—Y—F wherein N is a nucleoside polyphosphate or analog thereof; F is adetectable label moiety; and Y comprises a polymerase interactinglinkage complex comprising a polymerase interacting group positionedfrom 20 to 40 angstroms from a nucleoside portion of the nucleosidepolyphosphate; and monitoring reaction of the nucleotide compositionwith the complex in a primer extension reaction by detecting a signalfrom the detectable label.
 13. The method of claim 12, wherein thenucleotide composition is selected from the group:

and wherein R₁ through R₁₁ are independently selected from H, O, OH,positively charge groups and negatively charged groups, and L₁ is afirst linker group, and, L₂ is a second linker group.
 14. The method ofclaim 13, wherein R₁ through R₁₁ are independently selected from H, O,OH, guanidinium, amine, ammonium, iminium, oxonium, carboxyl, phosphate,phosphonate, thio, sulfate, sulfonate, thioate, and phosphothioate. 15.The method of claim 13, wherein the polymerase interacting linkagecomplex comprises one or more hydrophobic groups selected from phenyl,biphenyl, triphenyl and coumarin derivative groups.
 16. The method ofclaim 15, wherein the one or more hydrophobic groups is selected from achromene, 2-chromanone, 2H-chromene, or 2H-chromen-2-none group.
 17. Themethod of claim 12, wherein the complex is immobilized upon a solidsupport.
 18. The method of claim 12, wherein the polymerase interactinglinkage complex (Y) comprises the structure:-L₁-P-L₂- where L₁ is a first linker group, P is a polymeraseinteracting group, and L₂ is a second linker group.
 19. The method ofclaim 12, wherein the polymerase interacting linkage complex (Y)comprises the structure:

where L₁ is a first linker group, P′ is a polymerase interacting group,L₂ is a second linker group, and X is a linking group.
 20. Thenucleotide composition of claim 12, wherein the polymerase interactingcomponent comprises a hydrophobic group having one or more phenylgroups.